rs1057517717

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(-;-)	0	common in clinvar

Make rs1057517717(-;A)

Make rs1057517717(A;A)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

85894260

Gene

CHM

is a	snp
is	mentioned by
dbSNP	rs1057517717
dbSNP (classic)	rs1057517717
ClinGen	rs1057517717
ebi	rs1057517717
HLI	rs1057517717
Exac	rs1057517717
Gnomad	rs1057517717
Varsome	rs1057517717
LitVar	rs1057517717
Map	rs1057517717
PheGenI	rs1057517717
Biobank	rs1057517717
1000 genomes	rs1057517717
hgdp	rs1057517717
ensembl	rs1057517717
geneview	rs1057517717
scholar	rs1057517717
google	rs1057517717
pharmgkb	rs1057517717
gwascentral	rs1057517717
openSNP	rs1057517717
23andMe	rs1057517717
SNPshot	rs1057517717
SNPdbe	rs1057517717
MSV3d	rs1057517717
GWAS Ctlg	rs1057517717

Max Magnitude

0

ClinVar
Risk	rs1057517717(A;A)
Alt	rs1057517717(A;A)
Reference	Rs1057517717(-;-)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CHM
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.85149266dupT
CLNSRC
CLNACC	RCV000412929.1,